The phrase "a common interaction of" is correct and usable in written English.
It can be used to describe a frequent or typical way in which two or more elements engage or relate to each other.
Example: "The study focused on a common interaction of social media and mental health among teenagers."
Alternatives: "a typical engagement of" or "a frequent relationship of".
In fact, if a complete or partial pathway is directly associated with an interaction or process it will always turn up, if the connection is looser (two or more mediating functions); this is only the case if all components are member of a common interaction network or part of an overarching process.
Although there is a high frequency of glycine and small residues in the 58 TM helix sequences of the human RTKs, direct conservation of a common interaction motif is not apparent.
While integration on the user interface level is desirable both from a software engineering as well as from a usability point of view, most current approaches require detailed knowledge of the integrated applications and make the implementation of a common interaction that involves different applications a difficult issue.
In addition, CLN1 and CLN5 share a common interaction partner, the F1 subunit of ATP synthase, which modulates the lipid homeostasis in neurons (Lyly et al., 2008; Lyly et al., 2009).
The circularization is thought to be caused by the common interaction of the cap-binding protein eIF4E and the polyA tail binding protein (PABP) with the scaffolding protein eIF4G.
We also confirmed the common interaction of LNX1, LNX2 and MUPP1 with EphA7 and show that EphA7 can bind, not only to an isolated LNX1 PDZ domain [ 42], but also to full-length LNX2 and near full-length LNX1 proteins.
When comparing different networks a network similarity (NS) measure was devised: where A and B represents different networks, SAB the similarity (i.e. the frequency of common interactions) of A versus B, and SBA the similarity of B versus A. Networks were visualized using Biolayout [ 66] and Cytoscape [ 67].
Finally, Tanrikulu et al. used a structure-based pharmacophore model based on the common interactions of four PPARγ X-ray crystal structures in complex with different agonists [143].
